A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497437



Internal ID20870643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56626953..56633824hg38UCSC Ensembl
chr16:56660865..56667736hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg386872
hg196872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192751
Samples
Known GenesMT1E, MT1M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497437
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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